Failure of first meningococcal vaccination in patients with atypical haemolytic uraemic syndrome treated with eculizumab

被引:24
作者
Gaeckler, Anja [1 ]
Kaulfuss, Meike [2 ]
Rohn, Hana [2 ]
Vogel, Ulrich [3 ]
Claus, Heike [3 ]
Feldkamp, Thorsten [4 ]
Kribben, Andreas [1 ]
Witzke, Oliver [2 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Dept Nephrol, Essen, Germany
[2] Univ Duisburg Essen, Univ Hosp Essen, Dept Infect Dis, Essen, Germany
[3] Univ Wurzburg, Inst Hyg & Microbiol, Natl Reference Lab Meningococci & Haemophilus Inf, Wurzburg, Germany
[4] Christian Albrechts Univ Kiel, Univ Hosp Schleswig Holstein, Dept Nephrol & Hypertens, Kiel, Germany
关键词
atypical haemolytic uraemic syndrome; bactericidal titres; complement inhibition; immunosuppression; meningococcal vaccination; RENAL-TRANSPLANT RECIPIENTS; THROMBOTIC MICROANGIOPATHY; DISEASE; RECOMMENDATIONS; IMMUNOGENICITY; PREVENTION; ANTIBODY;
D O I
10.1093/ndt/gfy225
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background The C5 complement inhibitor eculizumab is a first-line treatment in atypical haemolytic uraemic syndrome (aHUS). Therapy with eculizumab is associated with a highly increased risk for meningococcal infection. Therefore, vaccination is highly recommended before beginning treatment. Efficacy of quadrivalent meningococcal vaccines (MenACWY) in patients treated with the C5 complement inhibitor eculizumab in aHUS has not yet been determined. Methods Patients with aHUS received one dose of a MenACWY conjugate vaccine before eculizumab treatment commenced. Bactericidal titres against meningococcal serogroups A, C, W and Y were determined using baby rabbit complement in 25 patients. Results Full immune response to meningococcal vaccination was detected in five patients (20%), while seven patients (28%) showed no immune response in any of the tested serogroups. The remaining 13 patients showed incomplete immune response with proof of protective antibody titres for one to three serogroups without perceptible preference for any serogroup. Bactericidal titres after re-vaccination were available for 17 patients. Nine patients with incomplete immune response after first vaccinations showed protective antibody titres for all serogroups after re-vaccination. Kidney function had improved in >50% of patients at the time of re-vaccination compared with the time of first vaccination and immunosuppressive therapy was only applied to re-vaccinated patients following kidney transplantation. Conclusions Immunogenicity of first quadrivalent meninongococcal vaccination is insufficient in patients with aHUS. Booster response is promising, but incomplete. Therefore, establishing antibiotic prophylaxes seems pivotal.
引用
收藏
页码:298 / 303
页数:6
相关论文
共 50 条
  • [1] Current evidence on the discontinuation of eculizumab in patients with atypical haemolytic uraemic syndrome
    Macia, Manuel
    de Alvaro Moreno, Fernando
    Dutt, Tina
    Fehrman, Ingela
    Hadaya, Karine
    Gasteyger, Christoph
    Heyne, Nils
    CLINICAL KIDNEY JOURNAL, 2017, 10 (03): : 310 - 319
  • [2] Eculizumab in secondary atypical haemolytic uraemic syndrome
    Cavero, Teresa
    Rabasco, Cristina
    Lopez, Antia
    Roman, Elena
    Avila, Ana
    Sevillano, Angel
    Huerta, Ana
    Rojas-Rivera, Jorge
    Fuentes, Carolina
    Blasco, Miquel
    Jarque, Ana
    Garcia, Alba
    Mendizabal, Santiago
    Gavela, Eva
    Macia, Manuel
    Quintana, Luis F.
    Maria Romera, Ana
    Borrego, Josefa
    Arjona, Emi
    Espinosa, Mario
    Portoles, Jose
    Gracia-Iguacel, Carolina
    Gonzalez-Parra, Emilio
    Aljama, Pedro
    Morales, Enrique
    Cao, Mercedes
    Rodriguez de Cordoba, Santiago
    Praga, Manuel
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2017, 32 (03) : 466 - 474
  • [3] Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab
    Chonat, Satheesh
    Chandrakasan, Shanmuganathan
    Kalinyak, Karen Ann
    Ingala, David
    Gruppo, Ralph
    Kalfa, Theodosia A.
    BRITISH JOURNAL OF HAEMATOLOGY, 2016, 175 (04) : 744 - 747
  • [4] Early treatment with eculizumab in atypical haemolytic uraemic syndrome
    Garjau, Maria
    Azancot, Maria
    Ramos, Rosa
    Sanchez-Corral, Pilar
    Angeles Montero, Maria
    Seron, Daniel
    CLINICAL KIDNEY JOURNAL, 2012, 5 (01) : 31 - 33
  • [5] Eculizumab: A Review of Its Use in Atypical Haemolytic Uraemic Syndrome
    Gillian M. Keating
    Drugs, 2013, 73 : 2053 - 2066
  • [6] A systematic review of eculizumab for atypical haemolytic uraemic syndrome (aHUS)
    Rathbone, John
    Kaltenthaler, Eva
    Richards, Anna
    Tappenden, Paul
    Bessey, Alice
    Cantrell, Anna
    BMJ OPEN, 2013, 3 (11):
  • [7] Eculizumab: A guide to its use in atypical haemolytic uraemic syndrome
    Keating G.M.
    Drugs & Therapy Perspectives, 2014, 30 (5) : 166 - 172
  • [8] Novel aspects of atypical haemolytic uraemic syndrome and the role of eculizumab
    Verhave, Jacobien C.
    Wetzels, Jack F. M.
    van de Kar, Nicole C. A. J.
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2014, 29 : 131 - 141
  • [9] Atypical haemolytic uraemic syndrome and pregnancy: outcome with ongoing eculizumab
    Servais, Aude
    Devillard, Nadege
    Fremeaux-Bacchi, Veronique
    Hummel, Aurelie
    Salomon, Laurent
    Contin-Bordes, Cecile
    Gomer, Helene
    Legendre, Christophe
    Delmas, Yahsou
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 (12) : 2122 - 2130
  • [10] Atypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: the experience of the Australian compassionate access cohort
    Mallett, A.
    Hughes, P.
    Szer, J.
    Tuckfield, A.
    Van Eps, C.
    Cambell, S. B.
    Hawley, C.
    Burke, J.
    Kausman, J.
    Hewitt, I.
    Parnham, A.
    Ford, S.
    Isbel, N.
    INTERNAL MEDICINE JOURNAL, 2015, 45 (10) : 1054 - 1065